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Tenon Medical

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2026-04-08

SEC Filings: 1 filings on record. Latest: 8-K (2026-08-24). View on SEC EDGAR →

TypeNumberDevice NameCodeDateActions
510(k) K260477 CATAMARAN™ SI Joint Fusion SystemOUR2026-04-08 View
510(k) K250403 Catamaran SI Joint Fusion SystemOUR2025-03-21 View
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